Polymerase chain reaction (PCR) techniques development allows the elaboration of many assays for identification of bacteria's resistance mechanisms to antibiotics. Following this idea, the results of molecular level investigation of bacteria's resistance mechanisms to antibiotics may give many opportunities to find more rapid methods for identifying the genes which are responsible for antibiotic resistance induction. The aim of the current study was to investigate antibiotic resistance genes in Staphylococcus bacteria on molecular level. Among classes of antibiotics, macrolides-lincosamides-streptogramin B (MLSB) and beta-lactams were used. In the proposed study, the bacterial strains were represented by 50 isolates of Staphylococcus. The bacterial strains were analyzed using polymerase chain reaction to identify the nuc, tuf, tst, sea, pathogenic activity genes. Thereafter, the bacteria were tested for ermA, ermB, ermC genes and for mecA, femA which are involved in the resistance to macrolides, lincosamides, streptogramin B and to beta-lactams, respectively. The presence or the absence of these genes confirmed that tested strains are resistant to specific antibiotic or not. Bacteria pathogenic activity was emphasized by genes as follows: sea (enterotoxin) which was found at all isolates, tst (toxic shock toxin) gene was not detected in any of the isolates and tuf gene (elongation factor) was obtained with one pair of primers. Resistance to beta-lactams was evidenced by the presence of mecA in all isolates and femA in some strains. Each of ermC, ermA and ermB, macrolides-lincosamides-streptogramin B resistance genes, was detected.